ClinVar Miner

Submissions for variant NC_000023.10:g.(?_154689387)_(154776950_?)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
The Central Laboratory of Birth Defects Prevention and Control, The Affiliated Women and Children's Hospital of Ningbo University RCV004768480 SCV005382013 uncertain significance Hereditary factor VIII deficiency disease 2024-09-30 criteria provided, single submitter clinical testing Variant summary: The CNV identified by Oxford Nanopore sequencing and optical genome mapping involves 87.56Kb duplication, including a partial int22h3 and TMLHE exon 2-8. Although exact breakpoints of this duplication are not known, the CNV inserted int22h1 of the F8 gene and expected to result in isolation of F8 gene, a known mechanism of disease (PMID: 30088696). No submitters have reported clinical-significance assessments for this CNV to ClinVar. According to the ACMG, the CNV of F8 is a variant of uncertain significance (1A, 2I (Scoring: 0.3), 3A, 5D(Scoring: 0.45))(PMID: 31690835).

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